Abstract

BackgroundLymphogranuloma venereum (LGV) proctitis is caused by Chlamydia trachomatis (Ct) genotype L and is endemic among men who have sex with men (MSM) in western society. Genotype L infections need to be distinguished from non-LGV (genotypes A-K) Ct infections since they require prolonged antibiotic treatment. For this purpose, an in-house developed pmpH based LGV polymerase chain reaction (PCR) test is used at the Amsterdam STI outpatient clinic. We investigated retrospectively the anal Ct genotype distribution, and the frequency of concomitant genotype infections in MSM infected with LGV and non-LGV Ct infections. To detect concomitant Ct genotype infections, the pmpH LGV PCR and genoTyping Reverse Hybridization Assay (Ct-DT RHA) were used.MethodsA total of 201 Ct positive rectal swabs from MSM were selected, which were previously diagnosed as either LGV (n = 99) or non-LGV Ct infection (n = 102) according to the algorithm of Ct detection by the commercially available Aptima Combo 2 assay followed by an in-house pmpH LGV PCR. The samples were retested with the commercially available Ct-DT RHA, which differentiates between 14 major genotypes and is able to detect concomitant Ct genotypes.ResultsExcellent genotyping agreement was observed between the Ct-DT RHA and the pmpH LGV PCR (Kappa = 0.900, 95%CI = 0.845-0.955, McNemar's p = 1.000). A concomitant non-LGV genotype was detected in 6/99 (6.1%) LGV samples. No additional LGV infections were observed with the Ct-DT RHA among the non-LGV Ct group. In the non-LGV group genotype G/Ga (34.3%) was seen most frequent, followed by genotype D/Da (22.5%) and genotype J (13.7%). All LGV infections were caused by genotype L2.ConclusionsConcomitant non-LGV genotypes do not lead to missed LGV proctitis diagnosis. The pmpH LGV PCR displayed excellent agreement with the commercially available Ct-DT genotyping RHA test. The genotypes G/Ga, D/Da and J were the most frequent non-LGV Ct strains in MSM.

Highlights

  • Lymphogranuloma venereum (LGV) proctitis is caused by Chlamydia trachomatis (Ct) genotype L and is endemic among men who have sex with men (MSM) in western society

  • We evaluated the diagnostic performance of the pmpH LGV polymerase chain reaction (PCR), used at the MHS of Amsterdam for the diagnosis of LGV infections, by retesting 100 LGV Ct positive and 100 non-LGV Ct positive samples with the Ct-Detection and genoTyping (DT) reverse hybridization assay (RHA) PCR system

  • Agreement between the Ct-DT RHA and the pmpH LGV PCR An excellent agreement was observed between the Ct-DT RHA and the pmpH LGV PCR in differentiating between an LGV and a non-LGV Ct infection (Kappa value = 0.900, 95% CI = 0.845 - 0.955, McNemar’s p = 1.000) (Table 1). 189/201 (94%) samples showed diagnostic concordance between the two assays, consisting of 91 LGV infections, 82 non-LGV infections, 4 mixed LGV/non-LGV infections and 12 non-typable infections

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Summary

Introduction

Lymphogranuloma venereum (LGV) proctitis is caused by Chlamydia trachomatis (Ct) genotype L and is endemic among men who have sex with men (MSM) in western society. Genotype L infections need to be distinguished from non-LGV (genotypes A-K) Ct infections since they require prolonged antibiotic treatment. For this purpose, an in-house developed pmpH based LGV polymerase chain reaction (PCR) test is used at the Amsterdam STI outpatient clinic. In men who have sex with men (MSM), the rectum is often the only infected site, without a concurrent Ct. In general, Ct infections caused by non-LGV Ct genotypes (D-K) give few or no symptoms since they remain confined to the mucosal lining and do not trigger overt immunological reactions [4]. Nowadays several assays are available to differentiate between an LGV genotype and a non-LGV genotype [7,8,9,10,11]

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